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L-Methionine, N-(diphenylphosphino)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342654-79-9

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342654-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342654-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,5 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 342654-79:
(8*3)+(7*4)+(6*2)+(5*6)+(4*5)+(3*4)+(2*7)+(1*9)=149
149 % 10 = 9
So 342654-79-9 is a valid CAS Registry Number.

342654-79-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-diphenylphosphinomethionine methyl ester

1.2 Other means of identification

Product number -
Other names (S)-diphenylphosphinomethionine methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:342654-79-9 SDS

342654-79-9Downstream Products

342654-79-9Relevant academic research and scientific papers

Novel chiral phosphine ligands and complexes from amino acid esters

Slawin, Alexandra M.Z.,Woollins, J. Derek,Zhang, Qingzhi

, p. 621 - 632 (2007/10/03)

N-Diphenylphosphinoamino acid methyl/ethyl esters RCH(NHPPh2)CO2R′ la-le were prepared in high yield from equimolar amounts of amino acid methyl/ethyl ester hydrochloride and chlorodiphenylphosphine. The reaction proceeds with configurational retention. Oxidation of la (R = R′ = CH3) with H2O2 or S8 leads to the N-diphenyl-phosphinoylalanine methyl ester 2a or N-diphenylthiophosphinoylalanine methyl ester 3a. la-le function as monodentate ligands to [PtC12(cod)], [RhCl(cod)]2 and [AuCl(tht)] to give cis-[PtC12(1-P)2], [RhCl(cod)(1-P)] and [AuCi(1-P)]. Two equivalents of chlorodiphenylphosphine react with alanine methyl ester hydrochloride in CH2C12 to give N,N-bis(diphenylphosphino)alanine methyl ester, bdppal. This is an excellent bidentate ligand, the chelate complexes [MC12(bdppal-P,P′)] (M =Pd or Pt) being prepared and studied by X-ray analysis. Oxidation at one P atom in bdppal with either H2O2 or S8 gives N-diphenylphosphino-N-diphenylphosphinoylalanine methyl ester, bdppalO, and N-diphenylphosphino-N-diphenylthiophosphinoylalanine methyl ester, bdppalS, respectively, bdppalO is very difficult to isolate but does react in situ with [PdC12(cod)] to give [PdC12(bdppalO-O,P)]. bdppalS reacts with [MCl2(cod)] (M = Pd or Pt) giving [MC12(bdppalS-P,S)]. The dioxidised product N,N-bis(diphenylphosphinoyl)alanine methyl ester, bdppalO2, does not react with [MC12(cod)] (M =Pd or Pt), whereas N,N-bis(diphenylthiophosphinoyl)alanine methyl ester, bdppalS2, reacts with [PdC12(cod)] to give [PdC12(bdppal-S,S′)]. All the compounds are chiral and have been fully characterised by microanalysis, IR, 31P-{1H}, 1H NMR, and FAB+ mass spectroscopies, and in several cases structures are confirmed by X-ray analysis. The crystal structures described and those previously determined reveal the configurational retention of the reactions.

New chiral ligands and complexes from α-amino acids

Zhang, Qingzhi,Slawin, Alexandra M. Z.,Woollins, J. Derek

, p. 215 - 218 (2007/10/03)

N-diphenylphosphinoamino methyl/ethyl esters, dppam, react with [PtCl2(cod)] and [RhCl(cod)]2 to give cis-[PtCl2(dppam-P)2] and [RhCl(cod)(dppam-P], while interaction of dppam with [PdCl2(cod)] leads

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